Nexome (RUO)

Next-generation sequencing testing kit for comprehensive genomic analysis and variant detection. Enables high-throughput sequencing for applications in molecular diagnostics and research.

Next Generation Sequencing platform for comprehensive genomic and molecular analysis. This advanced sequencing technology enables high-throughput analysis of DNA and RNA samples.

A semi-automated kit for next-generation sequencing (NGS) of the exonic regions of the human genome, covering a 37.64 Mb region using genomic DNA extracted from whole blood and buccal swabs. The kit includes reagents for the preparation of DNA libraries enriched in exonic regions, intended for use on Illumina NGS sequencing platforms. It is designed for the identification of genetic variants in the exome to support the diagnosis of hereditary diseases, detect variants related to disease predisposition, and guide personalized medicine.

Comprehensive gene sequencing preparation kit targeting exon regions for clinical genomic analysis. Designed for targeted genetic profiling and diagnostic applications.

End-to-end next-generation sequencing support on Illumina, MGI, and compatible NGS platforms. Services encompass library preparation, sequencing, and data quality control processes for comprehensive genomic analysis.

Genomic sequencing panel for cancer-related mutation and biomarker detection. Supports precision oncology treatment planning and selection.

Kit for preparation of next-generation sequencing libraries covering the entire human exome and mitochondrial genome. Designed for comprehensive genomic analysis applications requiring high-throughput sequencing capabilities.

Next-generation sequencing diagnostic kits developed and manufactured for genomic analysis and sequencing applications. Provides complete kit solutions including reagents, components, and assembly with full GMP compliance.

Reagents and reagent kits for genomic analysis and next-generation sequencing applications. These products support whole genome and targeted sequencing research workflows.

High-throughput DNA sequencing service for clinical sample analysis and genomic profiling. This service enables identification of disease-associated genetic variants for precision medicine applications.

Next-generation sequencing services for research and diagnostic applications including metagenomic profiling, viral surveillance, and molecular analysis. Supported by specialized collection kits and purification protocols.

Next-generation sequencing panel for comprehensive cancer genomic profiling. Identifies mutations, copy number variations, and other genetic alterations to guide personalized treatment strategies.